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Name:Bactimicina Allergy
Manufacturer:Dlc Laboratories, Inc.
Category:Over-the-counter (OTC) Marketed Drugs


BACTIMICINA FOR ALLERGY LORATADINE 10 MG/ANTIHISTAMINE

BACTIMICINA ALLERGY   - loratadine tablet 
DLC Laboratories, Inc.

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BACTIMICINA FOR ALLERGY LORATADINE 10 MG/ANTIHISTAMINE

Active ingredient (in each tablet)

Loratadine USP, 10mg

Purpose

Antihistamine


Uses

temporarily relieves these symptoms due to hay fever or other respiratory allergies:

  • runny nose
  • itchy, watery eyes
  • sneezing
  • itching of the nose or throat

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

When using this product do not take more than directed. Taking more than directed may cause drowsiness.


If pregnant or breast feeding, ask a health professional before use.

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions


adults and children 6 years and over            1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of age                        ask a doctor
consumers with liver or kidney disease          ask a doctor

Other information

TAMPER EVIDENT; DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING

  • see side panel for lot number and expiration date
  • store between 20 and 25 degrees C (68 and 77 degrees F)
  • protect from excessive moisture

Inactive ingredients

corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

Questions or Comments?

 1-800-858-3889

Distributed by:
DE LA CRUZ PRODUCTS

A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA
www.dlclabs.com

Package Labeling

Bactimicina Allergy

Bactimicina Allergy


BACTIMICINA ALLERGY  
loratadine tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:24286-1549
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LORATADINE (LORATADINE) LORATADINE 10 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN  
LACTOSE MONOHYDRATE  
MAGNESIUM STEARATE  
Product Characteristics
Color white (White) Score no score
Shape ROUND (RX526) Size 7mm
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:24286-1549-2 2 BLISTER PACK ( BLISTER PACK) in 1 BOX contains a BLISTER PACK
1 10 TABLET ( TABLET) in 1 BLISTER PACK This package is contained within the BOX (24286-1549-2)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076134 10/21/2009

Labeler - DLC Laboratories, Inc. (093351930)

Revised: 05/2011 DLC Laboratories, Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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